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Platelets Poison Parasites Activated platelets bound to malaria parasite–infected red blood cells were once thought to contribute to pathogenesis, but recently the platelets have been found to have a protective effect. McMorran et al. (p. 1348 ; see the Perspective by Engwerda and Good ) extended this discovery to show that platelet activation releases intracellular granules containing a chemokine, PF4, which is internalized by Plasmodium falciparum –infected red cells. Subsequently, mature parasites within the cells die. The Duffy blood-group factor on red blood cells is known to act as a nonspecific receptor for chemokines, such as PF4, as well as a receptor for cell invasion by other species of malaria parasite. When the Duffy antigen was blocked by antibody treatment, platelets and PF4 were less able to kill the P. falciparum parasites within.
Blood Platelets, Erythrocytes, Plasmodium falciparum, cell organelle, malaria, Receptors, Cell Surface, genetic analysis, Platelet Factor 4, antigen, Humans, molecular analysis, Malaria, Falciparum, Keywords: Duffy binding protein, Cells, Cultured, protozoan, article, thrombocyte factor 4, host-parasite interaction, inhibition, Recombinant Proteins, gene expression, antigen expression, priority j, Duffy Blood-Group System
Blood Platelets, Erythrocytes, Plasmodium falciparum, cell organelle, malaria, Receptors, Cell Surface, genetic analysis, Platelet Factor 4, antigen, Humans, molecular analysis, Malaria, Falciparum, Keywords: Duffy binding protein, Cells, Cultured, protozoan, article, thrombocyte factor 4, host-parasite interaction, inhibition, Recombinant Proteins, gene expression, antigen expression, priority j, Duffy Blood-Group System
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